Canonical Allele Identifier: PA2825666911
Gene: SGCD HGNC NCBI

Linked Data

ClinVar Variation Id: 968720
ClinVar RCV Id: RCV001243920 RCV002499411 RCV003142216 RCV003234013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121681.1:p.Ser150Phe
CA3530600
NM_001128209.2:c.449C>T